The Safety Rates Drug Report

Member Login
2004.Q1    2004.Q2    2004.Q3    2004.Q4    2005.Q1    2005.Q2    2005.Q3    2005.Q4    2006.Q1    2006.Q2    2006.Q3    2006.Q4    2007.Q1    2007.Q2    2007.Q3    2007.Q4    2008.Q1    2008.Q2    2008.Q3    2008.Q4    2009.Q1    2009.Q2    2009.Q3    2009.Q4    2010.Q1    2010.Q2    2010.Q3    2010.Q4    2011.Q1    2011.Q2    2011.Q3    2011.Q4    2012.Q1    2012.Q2    2012.Q3    2012.Q4    2013.Q1    2013.Q2    2013.Q3    2013.Q4    2014.Q1    2014.Q2    2014.Q3    2014.Q4    2015.Q1    2015.Q2    2015.Q3    2015.Q4    2016.Q1    2016.Q2    2016.Q3   

Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
1165292818 11652928 18 F 2015 20160823 20151022 20160829 EXP CA-PFIZER INC-2015283489 PFIZER 52.00 YR F Y 0.00000 20160829 MD CA CA

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
1165292818 11652928 1 PS XELJANZ TOFACITINIB CITRATE 1 Oral 5 MG, 2X/DAY 203214 5 MG TABLET BID
1165292818 11652928 2 SS XELJANZ TOFACITINIB CITRATE 1 Oral 5 MG, 2X/DAY 203214 5 MG TABLET BID
1165292818 11652928 3 SS XELJANZ TOFACITINIB CITRATE 1 Oral 5 MG, 2X/DAY 203214 5 MG TABLET BID
1165292818 11652928 4 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Oral 15 MG, WEEKLY 11719 15 MG /wk
1165292818 11652928 5 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Oral 15 MG, WEEKLY 11719 15 MG /wk
1165292818 11652928 6 SS NAPROSYN NAPROXEN 1 UNK 0
1165292818 11652928 7 SS NAPROSYN NAPROXEN 1 2X/DAY 0 BID
1165292818 11652928 8 SS ATASOL ACETAMINOPHEN 1 UNK, AS NEEDED 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
1165292818 11652928 1 Rheumatoid arthritis
1165292818 11652928 4 Rheumatoid arthritis
1165292818 11652928 6 Pain
1165292818 11652928 8 Pain

Outcome of event

Event ID CASEID OUTC COD
1165292818 11652928 HO
1165292818 11652928 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
1165292818 11652928 Abdominal pain
1165292818 11652928 Chromaturia
1165292818 11652928 Condition aggravated
1165292818 11652928 Diarrhoea
1165292818 11652928 Drug effect incomplete
1165292818 11652928 Dysuria
1165292818 11652928 Eye pain
1165292818 11652928 Fatigue
1165292818 11652928 Haemorrhoids
1165292818 11652928 Incontinence
1165292818 11652928 Nail bed bleeding
1165292818 11652928 Nail infection
1165292818 11652928 Nasopharyngitis
1165292818 11652928 Pain in extremity
1165292818 11652928 Peripheral swelling
1165292818 11652928 Pollakiuria
1165292818 11652928 Pyrexia
1165292818 11652928 Urinary retention
1165292818 11652928 Uterine cancer
1165292818 11652928 Vaginal infection
1165292818 11652928 Vision blurred

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
1165292818 11652928 1 20150821 20151104 0
1165292818 11652928 2 20151109 20160315 0
1165292818 11652928 3 2016 0
1165292818 11652928 4 20160308 0
1165292818 11652928 5 2016 0